ATE502111T1 - GENE EXPRESSION IN PLASTIDS BASED ON REPLICATING VECTORS - Google Patents

GENE EXPRESSION IN PLASTIDS BASED ON REPLICATING VECTORS

Info

Publication number
ATE502111T1
ATE502111T1 AT02732689T AT02732689T ATE502111T1 AT E502111 T1 ATE502111 T1 AT E502111T1 AT 02732689 T AT02732689 T AT 02732689T AT 02732689 T AT02732689 T AT 02732689T AT E502111 T1 ATE502111 T1 AT E502111T1
Authority
AT
Austria
Prior art keywords
sequence
interest
selection marker
plastids
plant
Prior art date
Application number
AT02732689T
Other languages
German (de)
Inventor
Hans-Ulrich Koop
Stefan Muehlbauer
Sebastian Klaus
Christian Eibl
Fong-Chin Huang
Timothy Golds
Original Assignee
Icon Genetics Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Icon Genetics Gmbh filed Critical Icon Genetics Gmbh
Application granted granted Critical
Publication of ATE502111T1 publication Critical patent/ATE502111T1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8201—Methods for introducing genetic material into plant cells, e.g. DNA, RNA, stable or transient incorporation, tissue culture methods adapted for transformation
    • C12N15/8209—Selection, visualisation of transformants, reporter constructs, e.g. antibiotic resistance markers
    • C12N15/821—Non-antibiotic resistance markers, e.g. morphogenetic, metabolic markers
    • C12N15/8212—Colour markers, e.g. beta-glucoronidase [GUS], green fluorescent protein [GFP], carotenoid
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8201—Methods for introducing genetic material into plant cells, e.g. DNA, RNA, stable or transient incorporation, tissue culture methods adapted for transformation
    • C12N15/8209—Selection, visualisation of transformants, reporter constructs, e.g. antibiotic resistance markers
    • C12N15/821—Non-antibiotic resistance markers, e.g. morphogenetic, metabolic markers
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8201—Methods for introducing genetic material into plant cells, e.g. DNA, RNA, stable or transient incorporation, tissue culture methods adapted for transformation
    • C12N15/8214—Plastid transformation
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8242—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits
    • C12N15/8257—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits for the production of primary gene products, e.g. pharmaceutical products, interferon

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Molecular Biology (AREA)
  • Cell Biology (AREA)
  • Microbiology (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Plant Pathology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Magnetic Ceramics (AREA)

Abstract

A process of generating transgenic plants or plant cells transformed on their plastome and being devoid of a selection marker, comprising the following steps: (a) transforming plastids of a plant or plant cell with a DNA comprising: (i) a nucleotide sequence conferring replication of said DNA in a plant cell, (ii) at least one sequence of interest, (iii) sequences flanking said at least one sequence of interest necessary for stable integration of said at least one sequence of interest into the plastid genome, and (iv) a selection marker outside of said sequences flanking said sequence(s) of interest; (b) allowing integration of said at least one sequence of interest into the plastome in the presence of selective pressure; (c) allowing loss of said selection marker sequence by releasing selective pressure; and (d) recovering cells and/or plants being genetically transformed on their plastomes and being devoid of said selection marker.
AT02732689T 2001-07-06 2002-04-30 GENE EXPRESSION IN PLASTIDS BASED ON REPLICATING VECTORS ATE502111T1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10132780A DE10132780A1 (en) 2001-07-06 2001-07-06 Plastid gene expression via autonomously replicating vectors
PCT/EP2002/004777 WO2003004658A2 (en) 2001-07-06 2002-04-30 Gene expression in plastids based on replicating vectors

Publications (1)

Publication Number Publication Date
ATE502111T1 true ATE502111T1 (en) 2011-04-15

Family

ID=7690826

Family Applications (1)

Application Number Title Priority Date Filing Date
AT02732689T ATE502111T1 (en) 2001-07-06 2002-04-30 GENE EXPRESSION IN PLASTIDS BASED ON REPLICATING VECTORS

Country Status (9)

Country Link
US (1) US7371923B2 (en)
EP (1) EP1404848B1 (en)
JP (1) JP4340148B2 (en)
AT (1) ATE502111T1 (en)
AU (1) AU2002304711B2 (en)
CA (1) CA2453023C (en)
DE (2) DE10132780A1 (en)
MX (1) MXPA03011874A (en)
WO (1) WO2003004658A2 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10049587A1 (en) 2000-10-06 2002-05-02 Icon Genetics Ag Vector system for plants
DE10061150A1 (en) 2000-12-08 2002-06-13 Icon Genetics Ag Methods and vectors for the production of transgenic plants
DE10102389A1 (en) 2001-01-19 2002-08-01 Icon Genetics Ag Methods and vectors for plastid transformation of higher plants
DE10114209A1 (en) 2001-03-23 2002-12-05 Icon Genetics Ag Site-directed transformation using amplification vectors
DE10115507A1 (en) 2001-03-29 2002-10-10 Icon Genetics Ag Method for coding information in nucleic acids of a genetically modified organism
DE10121283B4 (en) 2001-04-30 2011-08-11 Icon Genetics GmbH, 80333 Methods and vectors for amplification or expression of desired nucleic acid sequences in plants
DE10132780A1 (en) 2001-07-06 2003-01-16 Icon Genetics Ag Plastid gene expression via autonomously replicating vectors
DE10143238A1 (en) 2001-09-04 2003-03-20 Icon Genetics Ag Identification of eukaryotic internal ribosome entry sites (IRES) elements
DE10143237A1 (en) 2001-09-04 2003-03-20 Icon Genetics Ag Manufacture of artificial internal ribosomal entry point elements (Ires elements)
DE10143205A1 (en) * 2001-09-04 2003-03-20 Icon Genetics Ag Process for protein production in plants
CN111819185A (en) 2017-12-15 2020-10-23 旗舰创业创新第六有限责任公司 Compositions comprising cyclic polyribonucleotides and uses thereof
WO2020198403A2 (en) 2019-03-25 2020-10-01 Flagship Pioneering Innovations Vi, Llc Compositions comprising modified circular polyribonucleotides and uses thereof

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US6147278A (en) 1985-10-25 2000-11-14 Monsanto Company Plant vectors
GB8626878D0 (en) 1986-11-11 1986-12-10 Ici Plc Dna
US5922602A (en) 1988-02-26 1999-07-13 Biosource Technologies, Inc. Cytoplasmic inhibition of gene expression
US6174700B1 (en) 1988-07-08 2001-01-16 University Of British Columbia Purification of a polypeptide compound having a polysaccharide binding domain by affinity phase separation
FR2649518B1 (en) 1989-07-07 1991-10-18 Bioprobe Systems Sa HIGH SECURITY ENCRYPTED MARKING METHOD AND DEVICE FOR THE PROTECTION OF VALUABLE OBJECTS
US5464764A (en) 1989-08-22 1995-11-07 University Of Utah Research Foundation Positive-negative selection methods and vectors
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DE10115507A1 (en) 2001-03-29 2002-10-10 Icon Genetics Ag Method for coding information in nucleic acids of a genetically modified organism
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DE10132780A1 (en) 2001-07-06 2003-01-16 Icon Genetics Ag Plastid gene expression via autonomously replicating vectors
DE10143237A1 (en) 2001-09-04 2003-03-20 Icon Genetics Ag Manufacture of artificial internal ribosomal entry point elements (Ires elements)
DE10143238A1 (en) 2001-09-04 2003-03-20 Icon Genetics Ag Identification of eukaryotic internal ribosome entry sites (IRES) elements
DE10143205A1 (en) 2001-09-04 2003-03-20 Icon Genetics Ag Process for protein production in plants

Also Published As

Publication number Publication date
US20050015829A1 (en) 2005-01-20
EP1404848B1 (en) 2011-03-16
CA2453023C (en) 2011-09-20
US7371923B2 (en) 2008-05-13
DE10132780A1 (en) 2003-01-16
DE60239462D1 (en) 2011-04-28
MXPA03011874A (en) 2004-06-03
JP4340148B2 (en) 2009-10-07
JP2004533266A (en) 2004-11-04
CA2453023A1 (en) 2003-01-16
AU2002304711B2 (en) 2007-04-05
WO2003004658A2 (en) 2003-01-16
WO2003004658A3 (en) 2004-01-08
EP1404848A2 (en) 2004-04-07

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